全文获取类型
收费全文 | 2919篇 |
免费 | 176篇 |
国内免费 | 4篇 |
出版年
2023年 | 9篇 |
2021年 | 29篇 |
2020年 | 31篇 |
2019年 | 47篇 |
2018年 | 71篇 |
2017年 | 47篇 |
2016年 | 78篇 |
2015年 | 134篇 |
2014年 | 154篇 |
2013年 | 194篇 |
2012年 | 249篇 |
2011年 | 246篇 |
2010年 | 163篇 |
2009年 | 123篇 |
2008年 | 194篇 |
2007年 | 192篇 |
2006年 | 132篇 |
2005年 | 150篇 |
2004年 | 157篇 |
2003年 | 87篇 |
2002年 | 88篇 |
2001年 | 73篇 |
2000年 | 75篇 |
1999年 | 61篇 |
1998年 | 18篇 |
1997年 | 18篇 |
1996年 | 15篇 |
1995年 | 21篇 |
1994年 | 10篇 |
1993年 | 7篇 |
1992年 | 16篇 |
1991年 | 20篇 |
1990年 | 10篇 |
1989年 | 10篇 |
1988年 | 8篇 |
1987年 | 10篇 |
1986年 | 6篇 |
1985年 | 5篇 |
1980年 | 5篇 |
1979年 | 8篇 |
1977年 | 5篇 |
1969年 | 4篇 |
1960年 | 4篇 |
1938年 | 4篇 |
1936年 | 9篇 |
1935年 | 5篇 |
1933年 | 8篇 |
1932年 | 9篇 |
1931年 | 9篇 |
1929年 | 7篇 |
排序方式: 共有3099条查询结果,搜索用时 31 毫秒
91.
As studies on vehicular ad hoc networks have been conducted actively in recent years, convenient and reliable services can be provided to vehicles through traffic information, surrounding information, and file sharing. To provide services for multiple requests, road side units (RSUs) should receive requests from vehicles and provide a scheduling scheme for data transfer according to priority. In this paper, we propose a new scheduling scheme by which multiple RSUs are connected through wired networks and data is transferred through the collaboration of RSUs. The proposed scheme transfers safety and non-safety data by employing a collaborative strategy of multiple RSUs as well as reducing the deadline miss ratio and average response time. When safety data is generated, data is transferred from the previous RSU in advance, while priority is assigned considering the deadline and reception rate. Since non-safety data is an on-demand data processed by user requests, the proposed scheme provides a method that reduces the deadline miss ratio upon loads generated in RSUs. To prove the superiority of the proposed scheme, we perform a performance evaluation in which the number and velocities of vehicles were changed. It is shown through the performance evaluation that the proposed scheme has better deadline miss ratios and faster response time than the existing schemes. 相似文献
92.
Yaxin Zhao Marta Vuckovic Hong Sik Yoo Nina Fox Adrienne Rodriguez Kyler McKessy Joseph L. Napoli 《The Journal of biological chemistry》2021,297(3)
The retinol dehydrogenase Rdh10 catalyzes the rate-limiting reaction that converts retinol into retinoic acid (RA), an autacoid that regulates energy balance and reduces adiposity. Skeletal muscle contributes to preventing adiposity, by consuming nearly half the energy of a typical human. We report sexually dimorphic differences in energy metabolism and muscle function in Rdh10+/− mice. Relative to wild-type (WT) controls, Rdh10+/− males fed a high-fat diet decrease reliance on fatty-acid oxidation and experience glucose intolerance and insulin resistance. Running endurance decreases 40%. Rdh10+/− females fed this diet increase fatty acid oxidation and experience neither glucose intolerance nor insulin resistance. Running endurance increases 220%. We therefore assessed RA function in the mixed-fiber type gastrocnemius muscles (GM), which contribute to running, rather than standing, and are similar to human GM. RA levels in Rdh10+/− male GM decrease 38% relative to WT. Rdh10+/− male GM increase expression of Myog and reduce Eif6 mRNAs, which reduce and enhance running endurance, respectively. Cox5A, complex IV activity, and ATP decrease. Increased centralized nuclei reveal existence of muscle malady and/or repair in GM fibers. Comparatively, RA in Rdh10+/− female GM decreases by less than half the male decrease, from a more modest decrease in Rdh10 and an increase in the estrogen-induced retinol dehydrogenase Dhrs9. Myog mRNA decreases. Cox5A, complex IV activity, and ATP increase. Centralized GM nuclei do not increase. We conclude that Rdh10/RA affects whole body energy use and insulin resistance partially through sexual dimorphic effects on skeletal muscle gene expression, structure, and mitochondria activity. 相似文献
93.
94.
Sang Kwang Lee Yongtae Kim Sung‐Soo Kim Jeong Hwa Lee Kun Cho Sang Sook Lee Zee‐Won Lee Kyung‐Hoon Kwon Young Hye Kim Haeyoung Suh‐Kim Jong Shin Yoo Young Mok Park 《Proteomics》2009,9(18):4389-4405
Mesenchymal stem cells (MSCs) are multipotent cells, which have the capability to differentiate into various mesenchymal tissues such as bone, cartilage, fat, tendon, muscle, and marrow stroma. However, they lose the capability of multi‐lineage differentiation after several passages. It is known that basic fibroblast growth factor (bFGF) increases growth rate, differentiation potential, and morphological changes of MSCs in vitro. In this report, we have used 2‐DE coupled to MS to identify differentially expressed proteins at the cell membrane level in MSCs growing in bFGF containing medium. The cell surface proteins isolated by the biotin–avidin affinity column were separated by 2‐DE in triplicate experiments. A total of 15 differentially expressed proteins were identified by quadrupole‐time of flight tandem MS. Nine of the proteins were upregulated and six proteins were downregulated in the MSCs cultured with bFGF containing medium. The expression level of three actin‐related proteins, F‐actin‐capping protein subunit alpha‐1, actin‐related protein 2/3 complex subunit 2, and myosin regulatory light chain 2, was confirmed by Western blot analysis. The results indicate that the expression levels of F‐actin‐capping protein subunit alpha‐1, actin‐related protein 2/3 complex subunit 2, and myosin regulatory light chain 2 are important in bFGF‐induced morphological change of MSCs. 相似文献
95.
Ai-hong Ji Hoon Cheol Park Quoc Viet Nguyen Jang Woo Lee Young Tai Yoo 《仿生工程学报(英文版)》2009,6(3):232-238
Ionic Polymer-Metal Composite (IPMC) can work as an actuator by applying a few voltages.A thick IPMC actuator,whereNafion-117 membrane was synthesized with polypyrrole/alumina composite filler,was analyzed to verify the equivalent beamand equivalent bimorph beam models.The blocking force and tip displacement of the IPMC actuator were measured with a DCpower supply and Young’s modulus of the IPMC strip was measured by bending and tensile tests respectively.The calculatedmaximum tip displacement and the Young’s modulus by the equivalent beam model were almost identical to the correspondingmeasured data.Finite element analysis with thermal analogy technique was utilized in the equivalent bimorph beam model tonumerically reproduce the force-displacement relationship of the IPMC actuator.The results by the equivalent bimorph beammodel agreed well with the force-displacement relationship acquired by the measured data.It is confirmed that the equivalentbeam and equivalent bimorph beam models are practically and effectively suitable for predicting the tip displacement,blockingforce and Young’s modulus of IPMC actuators with different thickness and different composite of ionic polymer membrane. 相似文献
96.
97.
98.
Sunkyung Lee Kyu Yang Yi Sung Jun Youn Byung Ho Lee Sung-eun Yoo 《Bioorganic & medicinal chemistry letters》2009,19(5):1329-1331
A series of (2-aryl-5-methylimidazol-4-ylcarbonyl)guanidines and (2-aryl-5-methyloxazol-4-ylcarbonyl)guanidines were synthesized and evaluated as NHE-1 inhibitors. The structure–activity relationships well matched those of furan derivatives, which were previously investigated. The (2,5-disubstituted)phenyl compounds showed better activities than the other analogues in both imidazole and oxazole compounds. Especially, 2-(2,5-dichlorophenyl)imidazole 52, and 2-(2-methoxy-5-chlorophenyl)imidazole 54 compounds exhibited potent cardioprotective efficacy both in vitro and in vivo as well as high NHE-1 inhibitory activities. 相似文献
99.
Ibrahim M. El-Deeb Byung Sun Park Su Jin Jung Kyung Ho Yoo Chang-Hyun Oh Seung Joo Cho Dong Keun Han Jae Yeol Lee So Ha Lee 《Bioorganic & medicinal chemistry letters》2009,19(19):5622-5626
A series of rationally designed ROS1 tyrosine kinase inhibitors was synthesized and screened. Compound 12b has showed good potency with IC50 value of 209 nM, which is comparable with that of the reference lead compound 1. Molecular modeling studies have been performed, that is, a homology model for ROS1 was built, and the screened inhibitors were docked into its major identified binding site. The docked poses along with the activity data have revealed a group of the essential features for activity. Overall, simplification of the lead compound 1 into compound 12b has maintained the activity, while facilitated the synthetic advantages. A molecular interaction model for ROS1 kinase and inhibitors has been proposed. 相似文献